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CAS 1310404-23-9

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B-(5-Fluoro-2-methyl-4-pyridinyl)boronic acid

Description:
B-(5-Fluoro-2-methyl-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has a fluorine and a methyl substituent. This compound typically exhibits properties such as being a white to off-white solid, with solubility in polar solvents like water and alcohols, which is common for boronic acids due to their ability to form hydrogen bonds. The presence of the fluorine atom can influence its reactivity and biological activity, making it a valuable intermediate in pharmaceutical synthesis and a potential ligand in various chemical reactions. Boronic acids are known for their ability to form reversible complexes with diols, which is significant in applications such as drug development and materials science. Additionally, this compound may exhibit specific biological activities, making it of interest in medicinal chemistry. Its unique structural features contribute to its utility in various synthetic pathways and applications in organic synthesis.
Formula:C6H7BFNO2
InChI:InChI=1S/C6H7BFNO2/c1-4-2-5(7(10)11)6(8)3-9-4/h2-3,10-11H,1H3
InChI key:InChIKey=XEKZLTJOECNOMJ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(F)=CN=C(C)C1
Synonyms:
  • B-(5-Fluoro-2-methyl-4-pyridinyl)boronic acid
  • Boronic acid, B-(5-fluoro-2-methyl-4-pyridinyl)-
  • (5-Fluoro-2-methylpyridin-4-yl)boronic acid
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